Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Alexandra Margaret Ure"'
Autor:
Eric Epping, Peggy Nopoulos, Anne Rosser, Nellie Georgiou-Karistianis, Stefan Klöppel, Roger Alistair Barker, Stacie Vik, Yongxia (Sharon) Zhou, Mirza Faisal Beg, Douglas Langbehn, Thomas Warner, Julie Stout, David Moser, Lynn Raymond, Ergun Uc, Anita Goh, Phyllis Chua, Hans Johnson, Kylie Radford, Thomas Wassink, Alexandra Margaret Ure, Charlotte Soneson, William Coryell, Carmela Pestell, WR Wayne Martin, Michael Hayden, Georg Bernhard Landwehrmeyer, Jane Paulsen, Vincent Magnotta
Publikováno v:
Neurobiology of Disease, Vol 40, Iss 3, Pp 531-543 (2010)
Huntington disease (HD) is a fatal neurodegenerative disorder caused by an expanded CAG repeat. Its length can be used to estimate the time of clinical diagnosis, which is defined by overt motor symptoms. Non-motor symptoms begin before motor onset,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b9b1556aa6f8f6b0bcd5f97f8c6b9ef
https://doi.org/10.1016/j.nbd.2010.07.013
https://doi.org/10.1016/j.nbd.2010.07.013
Autor:
Peggy Nopoulos, Anne Rosser, Nellie Georgiou-Karistianis, Stefan Klöppel, Roger Alistair Barker, Stacie Vik, Douglas Langbehn, Thomas Warner, Julie Stout, David Moser, Lynn Raymond, Ergun Uc, Anita Goh, Phyllis Chua, Hans Johnson, Kylie Radford, Alexandra Margaret Ure, William Coryell, WR Wayne Martin, Michael Hayden, Georg Bernhard Landwehrmeyer, Jane Paulsen, J. Timothy Greenamyre, Janet Karen Williams, Vincent Magnotta
Publikováno v:
Movement Disorders. 25:2595-2603
The basic aim of this study was to evaluate the current accepted standard clinical endpoint for the earliest-studied HD participants likely to be recruited into clinical trials. As the advent of genetic testing for HD, it is possible to identify gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::62311fd27fe1af2d0f90d054172de7c1
https://doi.org/10.1002/mds.23337
https://doi.org/10.1002/mds.23337